Canonical Allele Identifier: CA376859041

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199423T>G , CM000672.2:g.68199423T>G	GRCh38
NC_000010.10:g.69959180T>G , CM000672.1:g.69959180T>G	GRCh37
NC_000010.9:g.69629186T>G	NCBI36
NG_032118.1:g.98307T>G , LRG_410:g.98307T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3341T>G MANE Select	NP_115967.2:p.Leu1114Arg
ENST00000358913.10:c.3341T>G MANE Select	ENSP00000351790.5:p.Leu1114Arg
NM_001256267.1:c.3341T>G	NP_001243196.1:p.Leu1114Arg
NM_001256267.2:c.3341T>G	NP_001243196.1:p.Leu1114Arg
NM_001256268.1:c.2459T>G	NP_001243197.1:p.Leu820Arg
NM_001256268.2:c.2459T>G	NP_001243197.1:p.Leu820Arg
NM_032578.3:c.3341T>G , LRG_410t1:c.3341T>G	NP_115967.2:p.Leu1114Arg
NR_045662.3:n.2768T>G
NR_045662.4:n.2878T>G
NR_045663.3:n.3470T>G
NR_045663.4:n.3415T>G
ENST00000354393.6:c.2516T>G	ENSP00000346369.2:p.Leu839Arg
ENST00000354393.7:c.2516T>G	ENSP00000346369.2:p.Leu839Arg
ENST00000358913.9:c.3341T>G	ENSP00000351790.5:p.Leu1114Arg
ENST00000540630.5:c.3341T>G	ENSP00000441668.2:p.Leu1114Arg
ENST00000540630.6:c.3395T>G	ENSP00000441668.3:p.Leu1132Arg
ENST00000613327.4:c.2459T>G	ENSP00000480757.1:p.Leu820Arg
ENST00000613327.5:c.3341T>G	ENSP00000480757.2:p.Leu1114Arg
ENST00000688812.1:c.*604T>G	ENSP00000510658.1:n.*604T>G
ENST00000690544.1:c.*2612T>G	ENSP00000508989.1:n.*2612T>G
XM_006718043.2:c.3395T>G	XP_006718106.1:p.Leu1132Arg
XM_011540292.1:c.3371T>G	XP_011538594.1:p.Leu1124Arg
XM_017016833.1:c.3419T>G	XP_016872322.1:p.Leu1140Arg
XM_017016834.2:c.3341T>G	XP_016872323.1:p.Leu1114Arg
XM_024448236.1:c.2219T>G	XP_024304004.1:p.Leu740Arg
XR_946029.1:n.1804-148A>C